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Stereodynamics in NO(X) + Ar inelastic collisions.

Abstract:
The effect of orientation of the NO(X) bond axis prior to rotationally inelastic collisions with Ar has been investigated experimentally and theoretically. A modification to conventional velocity-map imaging ion optics is described, which allows the orientation of hexapole state-selected NO(X) using a static electric field, followed by velocity map imaging of the resonantly ionized scattered products. Bond orientation resolved differential cross sections are measured experimentally for a series of spin-orbit conserving transitions and compared with quantum mechanical calculations. The agreement between experimental results and those from quantum mechanical calculations is generally good. Parity pairs, which have previously been observed in collisions of unpolarized NO with various rare gases, are not observed due to the coherent superposition of the two j = 1/2, Ω = 1/2 Λ-doublet levels in the orienting field. The normalized difference differential cross sections are found to depend predominantly on the final rotational state, and are not very sensitive to the final Λ-doublet level. The differential steric effect has also been investigated theoretically, by means of quantum mechanical and classical calculations. Classically, the differential steric effect can be understood by considering the steric requirement for different types of trajectories that contribute to different regions of the differential cross section. However, classical effects cannot account quantitatively for the differential steric asymmetry observed in NO(X) + Ar collisions, which reflects quantum interference from scattering at either end of the molecule. This quantum interference effect is dominated by the repulsive region of the potential.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1063/1.4952649

Authors


More by this author
Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Sub department:
Physical & Theoretical Chem
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Role:
Author


More from this funder
Funding agency for:
Stolte, S
Grant:
91221301
11034003
More from this funder
Funding agency for:
Stolte, S
Grant:
91221301
11034003
More from this funder
Grant:
FP7 EU People ITN Project No. 238671
More from this funder
Grant:
CTQ2012-37404, CTQ2015-65033-P, CSD2009-00038


Publisher:
American Institute of Physics
Journal:
Journal of Chemical Physics More from this journal
Volume:
144
Issue:
22
Pages:
224301
Publication date:
2016-06-08
Acceptance date:
2016-05-09
DOI:
EISSN:
1089-7690
ISSN:
0021-9606


Language:
English
Pubs id:
pubs:628824
UUID:
uuid:1da30ee0-34c9-44dc-97d8-16b257174d09
Local pid:
pubs:628824
Source identifiers:
628824
Deposit date:
2016-06-20

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